Evidence map›Paper›PMID 42605346›Full record

ArticleRare tumors2026

Primary hepatic leiomyosarcoma diagnosed after right hepatectomy: A rare case report.

Toshikatsu Nitta, Masatsugu Ishii, Ryutaro Kubo, Akitada Sada, Atsuhiro Komiya, Atsushi Takeshita, Takashi Ishibashi

Abstract readCase Reports
In one paragraph

Article in Rare tumors, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Toshikatsu NittaDivision of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Osaka, Japan.ORCID https://orcid.org/0000-0001-6813-9584
Masatsugu IshiiDivision of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Osaka, Japan.
Ryutaro KuboDivision of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Osaka, Japan.
Akitada SadaDivision of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Osaka, Japan.
Atsuhiro KomiyaDivision of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Osaka, Japan.
Atsushi TakeshitaDepartment of Pathology, Medico Shunju Shiroyama Hospital, Osaka, Japan.
Takashi IshibashiDivision of Surgery Gastroenterological Center, Medico Shunju Shiroyama Hospital, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This is a case report of primary hepatic leiomyosarcoma. An 82-year-old Japanese man presented with fever and mild abdominal pain. Laboratory testing demonstrated marked inflammation and substantial elevations of CA19-9 and PIVKA-II. Computed tomography revealed a large necrotic mass in the right hepatic lobe with gallbladder wall thickening. Gallbladder cancer invading the liver with abscess formation was suspected, but a definitive preoperative diagnosis could not be established. Right hepatectomy and cholecystectomy achieved an R0 resection. Histopathological examination showed fascicles of spindle cells, extensive necrosis, and high mitotic activity. Immunohistochemical staining was positive for α-smooth muscle actin and h-caldesmon and negative for desmin and epithelial markers, confirming primary hepatic leiomyosarcoma. Although abscess-like presentations have been reported, the combination of severe inflammatory findings, markedly elevated CA19-9 and PIVKA-II, and gallbladder wall thickening was unusual and contributed to diagnostic confusion. This case emphasizes the need to consider primary hepatic leiomyosarcoma in the differential diagnosis of a large necrotic hepatic mass and supports complete surgical resection when technically feasible.

Indexed as

leiomyosarcomaliver tumorprimary hepatic leiomyosarcomarare tumorsright hepatectomy

Identifiers

PMID42605346
PMCPMC13477532

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